Fehime K. Eroglu
Ankara, Turkey
Last Updated: 09/26/2026
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Found 32 publications
Health-related quality of life in children with Familial Mediterranean Fever: a Pediatric Quality of Life Inventory-based evaluation with mutation-specific analysis.
Journal: European journal of pediatrics
Published: December 20, 2025
Predicting recalcitrant hyperinflammatory disease course in children with Kawasaki disease and MIS-C.
Journal: Pediatric rheumatology online journal
Published: December 13, 2025
Discovery of potent and selective inhibitors of human NLRP3 with a novel mechanism of action.
Journal: The Journal of experimental medicine
Published: December 17, 2024
S100A9 promotes inflammasome-dependent autoinflammation by blocking the degradation of SYK tyrosine kinase.
Journal: Journal of leukocyte biology
Published: November 26, 2024
Circulating extracellular vesicles of patients with steroid-sensitive nephrotic syndrome have higher RAC1 and induce recapitulation of nephrotic syndrome phenotype in podocytes.
Journal: American journal of physiology. Renal physiology
Published: September 27, 2021
Kidney disease profile and encountered problems during follow-up in Syrian refugee children: a multicenter retrospective study.
Journal: Pediatric nephrology (Berlin, Germany)
Published: October 18, 2020
Clinical characteristics of childhood acute tubulointerstitial nephritis.
Journal: Pediatrics international : official journal of the Japan Pediatric Society
Published: April 29, 2020
COL4A3 mutation is an independent risk factor for poor prognosis in children with Alport syndrome.
Journal: Pediatric nephrology (Berlin, Germany)
Published: February 26, 2020
An Extremely Rare Cause of Prolonged Menstruation: Lupus Anticoagulant-Hypoprothrombinemia Syndrome.
An Extremely Rare Cause of Prolonged Menstruation: Lupus Anticoagulant-Hypoprothrombinemia Syndrome.
Journal: Journal of obstetrics and gynaecology : the journal of the Institute of Obstetrics and Gynaecology
Published: September 04, 2019
Erratum to 'Response to early coenzyme Q10 supplementation is not sustained in CoQ10 deficiency caused by CoQ2 mutation' [Pediatric Neurology 88 (2018) 71-74].
Journal: Pediatric neurology
Published: February 20, 2019
MEFV gene mutations in children with Henoch-Schönlein purpura and their correlations-do mutations matter?
Journal: Clinical rheumatology
Published: January 20, 2019
Last Updated: 09/26/2026